Joseph Gladwin, Kelsey Rick G
Department of Forest Science, Oregon State University, Corvallis, OR 97331, USA.
J Exp Bot. 2004 May;55(399):1095-103. doi: 10.1093/jxb/erh116. Epub 2004 Mar 12.
Stem segments from terminal leaders of Douglas-fir, Pseudotsuga menziesii (Mirb.) Franco, seedlings were sampled in mid-December when cambial cells were dormant. The residual, debudded leaders were resampled again in early May when the cambium was metabolically active. May stems had higher constitutive ethanol concentrations than December stems. This was not the result of cambial hypoxia generated by rapid spring respiration rates, because when aerobic respiration was stimulated by incubating the stems in air at 30 degrees C ethanol production was induced in December, but not in May. Rapid respiration rates at 30 degrees C may have depleted O(2) supplies and induced ethanol production in December stems because dormant, thick-walled cambial cells may be less permeable to CO(2) and O(2), compared with metabolically active, thin-walled cambial cells in May. December stem segments incubated in a N(2) atmosphere at 30 degrees C synthesized 1.8 times more ethanol than segments from May, most likely because spring growth had reduced the soluble sugars available for fermentation. CO(2) efflux from May stems (after 5.5 h of incubation at 30 degrees C) was equal to December stems per unit volume, but greater than December stems per unit surface area. N(2)-induced ethanol concentrations were positively related with CO(2) efflux per unit volume, indicating that rapidly respiring leaders can maintain rapid fermentation rates, provided soluble sugars are readily available. N(2)-induced ethanol and CO(2) efflux per unit volume declined with increasing leader diameter in both seasons, whereas there were no relationships between CO(2) efflux per unit surface area and diameter. Cambium physiology and phenology influence the induction of fermentation and concentrations of ethanol produced in terminal leaders of Douglas-fir, and probably other conifers as well. This needs to be considered when comparing fermentation among species, or comparing individuals from different seasons, or disparate ages within a species.
在12月中旬,当形成层细胞处于休眠状态时,采集花旗松(Pseudotsuga menziesii (Mirb.) Franco)幼苗顶梢的茎段。在5月初,当形成层代谢活跃时,再次采集去除芽的剩余顶梢。5月的茎段组成型乙醇浓度高于12月的茎段。这不是春季呼吸速率快速导致形成层缺氧的结果,因为当将茎段在30℃空气中培养刺激有氧呼吸时,12月的茎段诱导产生了乙醇,而5月的茎段没有。30℃时的快速呼吸速率可能耗尽了12月茎段的氧气供应并诱导了乙醇产生,因为与5月代谢活跃的薄壁形成层细胞相比,休眠的厚壁形成层细胞对二氧化碳和氧气的渗透性可能较低。在30℃氮气气氛中培养的12月茎段合成的乙醇比5月茎段多1.8倍,很可能是因为春季生长减少了可用于发酵的可溶性糖。5月茎段(在30℃培养5.5小时后)的二氧化碳流出量按单位体积计算与12月茎段相等,但按单位表面积计算则大于12月茎段。氮气诱导的乙醇浓度与单位体积的二氧化碳流出量呈正相关,表明快速呼吸的顶梢只要可溶性糖容易获得就能维持快速发酵速率。两个季节中,单位体积的氮气诱导乙醇和二氧化碳流出量均随顶梢直径增加而下降,而单位表面积的二氧化碳流出量与直径之间没有关系。形成层生理和物候影响花旗松顶梢发酵的诱导以及产生的乙醇浓度,可能对其他针叶树也有影响。在比较物种间的发酵、不同季节的个体或同一物种内不同年龄的个体时,需要考虑这一点。